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Catalog Number:
32260
CAS Number:
34819-86-8
3,4-Di-O-acetyl-6-deoxy-L-glucal
Purity:
≥ 98% (HPLC)
Synonym(s):
Di-O-acetyl-L-rhamnal, 3,4-Di-O-acetyl-L-rhamnal
Documents
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Product Information

3,4-Di-O-acetyl-6-deoxy-L-glucal is a versatile chemical compound that serves as a valuable intermediate in the synthesis of various glycosides and oligosaccharides. This compound is particularly significant in carbohydrate chemistry, where it is utilized for the development of glycosyl donors, which are essential for the formation of glycosidic bonds in complex carbohydrates. Its unique structure, featuring acetyl groups, enhances its reactivity and stability, making it an ideal candidate for researchers focusing on carbohydrate synthesis and modification.

In the pharmaceutical and biotechnology industries, 3,4-Di-O-acetyl-6-deoxy-L-glucal is employed in the design of glycosylated drugs and biologically active compounds. Its ability to facilitate the introduction of sugar moieties into various molecules can lead to improved bioavailability and efficacy of therapeutic agents. Additionally, this compound is used in the development of diagnostic tools and vaccines, highlighting its broad applicability in both research and industrial settings. With its favorable properties and diverse applications, 3,4-Di-O-acetyl-6-deoxy-L-glucal is an essential resource for professionals engaged in carbohydrate chemistry and related fields.

Synonyms
Di-O-acetyl-L-rhamnal, 3,4-Di-O-acetyl-L-rhamnal
CAS Number
34819-86-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H14O5
Molecular Weight
214.22
MDL Number
MFCD00074970
PubChem ID
118189
Density
1.12
Appearance
Colorless to yellow liquid
Boiling Point
68 - 69 ?C / 0.06 mmHg
Refractive Index
n20/D 1.454
Optical Rotation
[a]20D = 55 ± 5 ° (C=1 in Chloroform)
Conditions
Store at 2 - 8 °C
General Information
Synonyms
Di-O-acetyl-L-rhamnal, 3,4-Di-O-acetyl-L-rhamnal
CAS Number
34819-86-8
Purity
≥ 98% (HPLC)
Molecular Formula
C10H14O5
Molecular Weight
214.22
MDL Number
MFCD00074970
PubChem ID
118189
Density
1.12
Appearance
Colorless to yellow liquid
Boiling Point
68 - 69 ?C / 0.06 mmHg
Refractive Index
n20/D 1.454
Optical Rotation
[a]20D = 55 ± 5 ° (C=1 in Chloroform)
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,4-Di-O-acetyl-6-deoxy-L-glucal is widely utilized in research focused on:

  • Synthesis of Glycosides: This compound serves as a key intermediate in the synthesis of various glycosides, which are important in pharmaceuticals and natural product chemistry.
  • Development of Antiviral Agents: Researchers explore its potential in creating antiviral compounds, contributing to the fight against viral infections.
  • Carbohydrate Chemistry: It plays a significant role in carbohydrate chemistry studies, helping scientists understand sugar interactions and modifications.
  • Bioconjugation Techniques: The compound is used in bioconjugation, allowing for the attachment of biomolecules to surfaces or other molecules, enhancing drug delivery systems.
  • Research in Enzyme Inhibition: It is investigated for its ability to inhibit specific enzymes, providing insights into metabolic pathways and potential therapeutic targets.

Citations